Molecular docking analysis of flavonoids with aldose reductase

被引:6
作者
Kannayiram, Kasthuri [1 ]
Umapathy, Vidhya Rekha [2 ]
Chamundeswari, Y. [3 ]
Fathima, J. H. [4 ]
Govindan, Ramajayam [5 ]
Palanisamy, Chella Perumal [6 ]
Veeraraghavan, Vishnu Priya [7 ]
Jayaraman, Selvaraj [7 ]
Rajagopal, Ponnulakshmi
机构
[1] Tagore Med Coll & Hosp, Dept Biochem, Chennai, Tamil Nadu, India
[2] Sree Balaji Dent Coll & Hosp, Dept Publ Hlth Dent, Chennai 600100, Tamil Nadu, India
[3] Dr MGR Educ & Res Inst, Allied Hlth Sci, Dept Biochem, Chennai, Tamil Nadu, India
[4] Ragas Dent Coll & Hosp, Dept Oral & Maxillofacial Pathol, Chennai, Tamil Nadu, India
[5] Madurai Med Coll, Multi Disciplinary Res Unit, Madurai, Tamil Nadu, India
[6] Qilu Univ Technol, Shandong Acad Sci, Coll Food Sci & Engn, State Key Lab Biobased Mat & Green Papermaking, Jinan 250353, Peoples R China
[7] Saveetha Univ, Saveetha Inst Med & Tech Sci, Saveetha Dent Coll & Hosp, Dept Biochem, Chennai, Tamil Nadu, India
关键词
Diabetes; molecular docking; aldose reductase; flavonoids; IN-VIVO; GLYCOSIDES;
D O I
10.6026/97320630018180
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Diabetes mellitus is a group of metabolic disorders that has risen to become the third most common cause in humans in recent years. The development of new bioactive substances from natural sources is a relatively new area. Flavonoids are believed to have a variety of beneficial properties in nature, including anti-inflammatory, antimicrobial, anticancer, antioxidant, neuroprotective, and anti-HIV properties. 15 naturally occurring flavonoids docked with the selected target aldose reductase. We report the optimal binding of Acumitin, Agathisflavone, Agehoustin B, and alpha-Toxicarol with aldose reductase for further consideration in drug discovery for T2DM.
引用
收藏
页码:180 / 183
页数:4
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